CN101993482A

CN101993482A - Protein associated with long grain foliaceous of paddy rice and coding gene and application thereof

Info

Publication number: CN101993482A
Application number: CN2009100917289A
Authority: CN
Inventors: 夏新界; 卢学丹
Original assignee: Individual
Current assignee: Individual
Priority date: 2009-08-24
Filing date: 2009-08-24
Publication date: 2011-03-30
Anticipated expiration: 2029-08-24
Also published as: RU2553206C2; JP2014236731A; ES2634187T3; IN2012DN01583A; CA2771927A1; US9434955B2; EP2471808A1; EP2471808B1; CA2771927C; BR112012008172A2; EP2471808A4; JP5938444B2; CN101993482B; US20120240292A1; RU2012108470A; JP2013502230A; WO2011022930A1

Abstract

The invention discloses a protein which is named as OsXCL and represented as (1) or (2): (1) protein consisting amino acid sequences represented by sequence 2 in a sequence list; and (2) protein derived from (1) substituted by and/or deleted with and/or added with one or more amino acids in the amino acid sequences in the sequence 2 of the sequence list and having the function of promoting long grain foliaceous of paddy rice. The invention further provides a coding gene of the protein. The grain weight of OsXCL transformed paddy rice obtained by introducing the coding gene in paddy rice achieves 4.224g and is increased by 25.1% compared with that of wild paddy rice and the grain is increased by 1/4.

Description

With relevant albumen and encoding gene and the application of paddy rice long grain leaf roll

Technical field

The present invention relates to biological technical field, particularly with relevant albumen and encoding gene and the application of paddy rice long grain leaf roll.

Background technology

Paddy rice is one of mankind's staple food crop of depending on for existence, and it is staple food with rice that the whole world has the population of half approximately.In China, rice yield occupies first of the food crop, and rice accounts for 60% in the consumption of resident's grain ration, and the peasant household that is engaged in the production of rice do is near 50% of peasant household's sum, and therefore, paddy rice occupies the leading position in China food crop.Continuous increase (rice country of consumption population speedup is faster than the average speedup of world population) along with global population, meanwhile owing to reasons such as the fast development of industrialization, urbanization, natural disaster damages, the rice field is reduces trend gradually, therefore, the disparities between supply and demand of world's rice will be more and more outstanding, how produce more grain to guarantee that the rice security provisions is face urgent of the whole world and the essential significant problem that solves on littler rice field area.But the output on the paddy rice big area is produced is all very low, and according to Food and Argriculture OrganizationFAO (FAO) statistics in 1999, the average per unit area yield of whole world paddy rice only is 3.8t.ha-1 (China is 6.3t.ha-1).For this reason, in nearly 30 years, China has successively proposed super high-yielding rice breeding plan (super hybridization rice breeding plan), excavates the yield potential of high-yield variety, reaches the purpose that significantly improves rice yield.Grain heavily is one of important factor that influences crop yield, and the big granule that increases grain is heavy, be one of some effective that improves rice yield, and the length of grain is the important morphological index of decision quality of rice.As when increasing output, can improve quality of rice again, then be our biologist, the agronomist institute target of pursuit the most.

Summary of the invention

The object of the present invention is to provide a kind of albumen, called after OsXCL derives from paddy rice, is following 1) or 2) albumen:

1) protein that the aminoacid sequence shown in the sequence 2 is formed in the sequence table;

2) in sequence table the aminoacid sequence of sequence 2 through replacement and/or disappearance and/or add one or several amino acid and with plant particle shape and leaf relevant by 1) deutero-protein.

Sequence table 2 is the aminoacid sequence of OsXCL, comprises 255 in amino acid, 72 of hydrophobic amino acids (comprising proline(Pro)), and 183 of hydrophilic amino acids, 34 of acidic amino acids, 38 of basic aminoacidss, protein molecular weight is: 26.73Kda, iso-electric point: 9.8.This protein is the new protein of not reported in the world.

In order to make 1) in OsXCL be convenient to purifying, label as shown in table 1 on proteinic N-terminal that can the aminoacid sequence shown in the sequence 2 is formed in by sequence table or C-terminal connect.

The sequence of table 1. label

Label	Residue	Sequence
			Poly-Arg	5-6 (being generally 5)	RRRRR
Poly-His	2-10 (being generally 6)	HHHHHH
			FLAG
	8	DYKDDDDK
			Strep-tag?II	8	WSHPQFEK
c-myc	10	EQKLISEEDL

Above-mentioned 2) but in the OsXCL synthetic, also can synthesize its encoding gene earlier, carry out biology again and express and to obtain.Above-mentioned 2) encoding gene of the OsXCL in can be by the codon with sequence in the sequence table 1 one or several amino-acid residue of disappearance in the dna sequence dna shown in 5 ' terminal the 106th to 870 bit base, and/or carry out the missense mutation of one or several base pair, and/or obtain at the encoding sequence that its 5 ' end and/or 3 ' end connects the label shown in the table 1.

Above-mentioned proteic encoding gene, called after OsXCL also belongs within protection scope of the present invention.

Above-mentioned encoding gene is following 1) or 2) or 3) or 4) gene:

1) encoding sequence be in the sequence table sequence 1 from the gene of 5 ' end shown in the 106th the-the 870th;

2) encoding sequence be in the sequence table sequence 1 from the gene of 5 ' end shown in the 50th the-the 873rd;

3) under the rigorous condition of height with 1) or 2) gene recombination that limits and the gene of encoding said proteins;

4) with 1) or 2) gene that limits has the homology more than 90% and the gene of encoding said proteins.

Sequence table 1 is the full-length cDNA of coding OsXCL.This sequence is altogether by 1062 based compositions, and wherein, the untranslated district of 5 ' end comprises 105 bases, the untranslated district of 3 ' end comprises 192 bases, the coding region is made up of 765 bases (from 106 to 870), and coding has the OsXCL albumen of the aminoacid sequence of sequence 2 in the sequence table, in the coding region, A accounts for 15.16% (116), C accounts for 40.65% (311), and G accounts for 32.29% (247), and T accounts for 11.9% (91), A+T accounts for 27.06% (207), and C+G accounts for 72.94% (558).

Above-mentioned high rigorous hybridization conditions is meant, with Hybond membrane place prehybridization solution (the 0.25mol/L sodium phosphate buffer, pH7.2,7%SDS) in, 65 ℃ of prehybridization 30min; Abandon prehybridization solution, add hybridization solution (0.25mol/L sodium phosphate buffer, pH7.2,7%SDS, isotope-labeled nucleotide fragments), 65 ℃ of hybridization 12hr; Abandon hybridization solution, (20mmol/L sodium phosphate buffer, pH7.2 5%SDS), wash film 2 times for 65 ℃, each 30min to add film washing liquid I; (20mmol/L sodium phosphate buffer, pH7.2 1%SDS), wash film 30min for 65 ℃ to add film washing liquid II.

Increase above-mentioned OsXCL full length gene or its arbitrary segmental primer to also belonging to protection scope of the present invention.

The transgenic cell line that contains said gene also belongs to protection scope of the present invention.

The reorganization bacterium that contains said gene also belongs to protection scope of the present invention.

The recombinant vectors that contains said gene also belongs to protection scope of the present invention.

Available existing plant expression vector construction contains the recombinant expression vector of OsXCL gene.Described plant expression vector comprises the double base agrobacterium vector and can be used for the carrier etc. of plant micropellet bombardment, as pCAMBIA3301, pCAMBIA1300, pBI121, pBin19, pCAMBIA2301, pCAMBIA1301-UbiN, pBY505 or other plant expression vector of deriving.When using the gene constructed recombinant expression vector of OsXCL, can before its transcription initiation Nucleotide, add any enhancement type, composing type, organizing specific type or inducible promoter, as cauliflower mosaic virus (CAMV) 35S promoter, ubiquitin (Ubiquitin) gene promoter (pUbi), Actin promotor etc., they can use separately or be used in combination with other plant promoter.

In addition, when using gene constructed plant expression vector of the present invention, also can use enhanser, comprise translational enhancer or transcriptional enhancer, these enhanser zones can be ATG initiator codon or neighboring region initiator codon etc., but must be identical with the reading frame of encoding sequence, to guarantee the correct translation of whole sequence.The source of described translation control signal and initiator codon is widely, can be natural, also can be synthetic.Translation initiation region can be from transcription initiation zone or structure gene.

For the ease of transgenic plant cells or plant being identified and screening, can process used plant expression vector, as be added in the plant to express and to produce the enzyme of colour-change or the gene of luminophor (gus gene, GFP gene, luciferase genes etc.), have the antibiotic marker thing (gentamicin marker, kantlex marker etc.) of resistance or anti-chemical reagent marker gene (as anti-weedkiller gene) etc.

Above-mentioned recombinant vectors specifically can be a multiple clone site of above-mentioned gene being inserted expression vector 163-1300, the recombinant vectors that obtains;

Wherein, the construction process of described expression vector 163-1300 is: pJIT163 is cut the DNA band that contains the Double 35S promoter that obtains with KpnI and XhoI enzyme and cut the big fragment that pCAMBIA1300 obtains through KpnI and SalI enzyme and be connected, obtain recombinant expression vector.

Another object of the present invention is to provide a kind of method of cultivating long grain leaf roll transgenic plant, is that above-mentioned gene is imported the purpose plant, obtains transgenic plant, and the grain length of these transgenic plant is greater than the purpose plant.

Another purpose of the present invention is to provide a kind of heavily method of the transgenic plant of increase of grain of cultivating, and is that the gene that the merchant states is imported the purpose plant, obtains transgenic plant, and the grain of described transgenic plant is great in described purpose plant.

Above-mentioned gene is to import in the purpose plant by above-mentioned recombinant vectors.Carry OsXCL gene of the present invention plant expression vector can by Ti-plasmids, Ri plasmid, plant viral vector, as particle bombardment, pollen tube channel, microinjection, electricity lead, conventional biological method such as agriculture bacillus mediated is transformed in vegetable cell or the tissue.

Above-mentioned plant is dicotyledons or monocotyledons; This monocotyledons specifically can be paddy rice.

Experimental results show that: the 100-grain weight of the commentaries on classics OsXCL paddy rice that the present invention cultivates reaches 4.224g, compares weightening finish 25.1% with the wild-type contrast; Grain increases by 1/4.Overexpression OsXCL in paddy rice causes that rice leaf is rolled, grain phenomenal growth, thousand seed weight significantly increase, rice matter improves.The application of OsXCL can increase output, can improve quality of rice again, without any negative impact, is comparatively ideal gene of crop such as biotechnology genetically engineered improvement paddy rice to rice growth, will play a positive role on the rice grain security is given birth to.

Description of drawings

Fig. 1 analyzes OsXCL cDNA that pcr amplification obtains figure as a result for agarose gel electrophoresis, and wherein, 1 is DNAmarker; 2,3 is OsXCL cDNA.

HindIII and EcoRI enzyme cut proof diagram to Fig. 2 behind the T carrier for OsXCL is connected to, and wherein, 1 is DNAmarker; 2-5 is the result of cloning vector behind EcoRI and HindIII double digestion of OsXCL cDNA.

Fig. 3 for OsXCL cDNA be connected to the T carrier after the BamHI enzyme cut checking; P1, P2, P3, P4 are the OsXCL cDNA plasmid bands before the BamHI enzyme is cut; 1, the 2,3, the 4th, the band of OsXCL cDNA plasmid after the BamHI enzyme is cut.

Fig. 4 is the collection of illustrative plates of pJIT163.

Fig. 5 is the collection of illustrative plates of pCAMBIA1300.

Fig. 6 is the part collection of illustrative plates that contains the pMD18-T carrier of OsXCL.

Fig. 7 for OsXCL be connected to expression vector after the EcoRI enzyme cut proof diagram, 1-5 cuts the result for the enzyme of the OsXCL expression vector of EcoRI enzyme after cutting.

Fig. 8 for OsXCL be connected to expression vector after the HindIII enzyme cut proof diagram, 1-5 is the OsXCL expression vector of HindIII enzyme after cutting.

Fig. 9 carries out EcoRI and HindIII single endonuclease digestion proof diagram respectively for extracting plasmid from Agrobacterium, and 1, DNAmarker; 2, the result of OsXCL expression vector plasmid after the EcoRI enzyme is cut; 3, the result of OsXCL expression vector plasmid after the HindIII enzyme is cut.

Figure 10 is for carrying out the PCR proof diagram according to hygromycin gene design primer, and wherein: M is DNA marker; 1-9,12-21 are the hygromycin gene PCR result that template is carried out to change OsXCL rice plant genomic dna; 10,22, be that template amplification Totomycin enzyme resistant gene is as positive control with the expression vector plasmid; 11,23, no template (water) negative control.

Figure 11 is non-transgenic contrast paddy rice for changeing OsXCL gene T0 for the quantitative real-time RT-PCR relative expression of 93-11 plant component analysis .S1; S2 is not for containing the empty carrier contrast paddy rice of OsXCL gene; S3-S25 is for changeing OsXCL gene T0 for the 93-11 rice plant

Figure 12 is for changeing OsXCL rice grain photo.

Figure 13 changes OsXCL paddy rice leaf photo.

Embodiment

The invention will be further described below in conjunction with specific embodiment, but the present invention is not limited to following examples.

Among the following embodiment, if no special instructions, be ordinary method.

Embodiment 1, the long grain of cultivation leaf roll transgenic paddy rice

One, the structure of recombinant expression vector

1, the clone of OsXCL gene

The a pair of primer of synthetic, and add NcoI and BamHI restriction enzyme site respectively at its 5 ' end.Upstream primer and downstream primer are as follows:

F：5-CCATGG?GAATCCAATCCACTCCACTCCACC-3(30)

R：5-GGATCC?CTAATAGGCGGTGTGGTGTTGCG-3(29)

Extract paddy rice and train the RNA in short 64S (rice in China cross-breeding center, China, Changsha), obtain article one chain of cDNA through reverse transcription.

With above-mentioned upstream primer and downstream primer is primer, and the cDNA that trains short 64S with paddy rice is a template, and pcr amplification goes out the cDNA shown in the sequence 1.The PCR condition is: 105 ℃ of heat lid temperature, and pre-94 ℃ of 5min of sex change, 94 ℃ of sex change 30s, 56 ℃ of annealing 30s, 72 ℃ are extended 1min20s, carry out 32 circulations; 72 ℃ are extended 10min, 22 ℃ of insulations.

The PCR system is:

ddH ₂O 3.25μl

2×GC?Buffer?I 12.5μl

Primer-1 (10 μ M) 2 μ l

Primer-2 (10 μ M) 2 μ l

dNTP 4μl

Template cDNA 1 μ l

LA Taq enzyme 0.25 μ l

Cumulative volume 25 μ l

Use the TAE electrophoretic buffer to carry out agarose gel electrophoresis, obtained the fragment (Fig. 1) about 800bp, called after OsXCL.

Above-mentioned OsXCL is taken back receipts, and the method for use is that the test kit extruding blob of viscose of TIANGEN reclaims.The fragment that reclaims is connected into pMD18-T carrier (TA Cloning, safe day of Jinan and bio tech ltd), and linked system is as follows:

Insert 4.5μl

T-Vector 0.5μl

Solution?I 5μl

Cumulative volume 10 μ l

Connect 2 hours, the competent cell of Transformed E .coli DH5 α, coated plate is with the screening of ammonia benzyl mycin.Select mono-clonal, identify that with HindIII and EcoRI double digestion the result all has the band of 800bp left and right sides OsXCL as shown in Figure 2 behind the extraction plasmid.

Direction when plasmid is cut checking purpose fragment OsXCL and is connected into the T carrier with the BamHI enzyme, the result is as shown in Figure 3: owing to added the site of BamHI on the downstream primer, just have band about 840bp if oppositely insert the T carrier, and the plasmid that P1, P2, P3, P4 representative are not cut among the figure, by the 1kb plus marker demonstration stripe size on right side.1, the result after 2,3,4 representatives are cut is by the 1kb plus marker demonstration stripe size on the left side.Results of comparison shows that 1,2, No. 3 plasmid also cuts except that No. 4 plasmids, and the purpose fragment all is that forward is connected into (promptly all being about 800bp).Bacterium liquid order-checking with 1,2, No. 3 correspondence, sequencing result show purpose fragment OsXCL be sequence 1 from 5 ' terminal 50-873 position, sequence 1 is in full accord from the sequence shown in 5 ' the terminal the 106th to 870 in the sequence of OsXCL gene ORF (Open reading frame, open reading frame) and the sequence table.

2, make up recombinant expression vector

1) structure of expression vector 163-1300

Cut as shown in Figure 4 pJIT163 (pGreen, http://www.pgreen.ac.uk/) with KpnI and XhoI enzyme, agarose gel electrophoresis is identified after enzyme is cut the result and is reclaimed the DNA band that contains the Double 35S promoter.PCAMBIA1300 (CambiaLabs, http://www.cambia.org/daisy/bioforge_legacy/3725.html) is as shown in Figure 5 cut with KpnI and SalI enzyme, reclaim big fragment.XhoI and SalI are isocaudarners, and two fragments that are recovered to connect with the T4 ligase enzyme spends the night, and is built into the 163-1300 complex carrier.

2) structure of recombinant expression vector

With as shown in Figure 6 the T carrier that contains OsXCL with enzyme NcoI and BamHI cut (no matter be BamHI effect be 872 restriction enzyme sites that design on restriction enzyme site that primers introduce or 887 the T carriers, the fragment that is recovered to has all comprised the terminator codon of OsXCL ORF), expression vector 163-1300 also cuts with these two enzymes, reclaiming the back connects, be about to gene OsXCL and be connected into expression vector 163-1300, constituted recombinant expression vector, called after OsXCL-163-1300, and distinguish single endonuclease digestion with HindIII and EcoRI and verify.The result is shown in Fig. 7 and Fig. 8 (1,2,3,4,5 represent the band of OsXCL expression vector after enzyme is cut respectively), and 1,3,4,5 all have the correct purpose band that contains the about 1600bp of OsXCL to produce.

Two, cultivate long grain leaf roll transgenic paddy rice and detection thereof

1, the acquisition of long grain leaf roll transgenic paddy rice

With the recombinant expression vector conversion Agrobacterium EHA105 (purchase in TIANGEN Biotech (Beijing) Co., Ltd.) of Agrobacterium freeze thawing conversion method with step 12.Extract plasmid from Agrobacterium and carry out EcoRI and HindIII single endonuclease digestion checking (Fig. 9).Wherein, the step of Agrobacterium freeze thawing conversion method is as follows:

Wherein the step of freeze-thaw method is as follows: take out the Agrobacterium EHA105 competent cell of-70 ℃ of preservations, ice bath melts; Get 10-20 μ l pCAMBIA1300-2 * CaMV35S-OsMsr1-CaMV35S-Term plasmid DNA (about 1-2 μ g), join in the Agrobacterium competent cell of 200ml thawing, stir evenly, left standstill several minutes with sterilization rifle head; Place liquid nitrogen 1min, 37 ℃ of water-bath 5min add 700-800 μ l LB liquid nutrient medium, 28 ℃, 200rpm, concussion 4h; 1000g 30sec removes the part supernatant, stays 100-150 μ l, inhales to beat again with the rifle head to suspend, and coats on the LB flat board that contains 50mg/L kantlex, 50mg/L Rifampin, 34mg/L paraxin, is inverted for 28 ℃ and cultivates 2d.

The Agrobacterium of the reorganization that above-mentioned empirical tests is crossed is infected the callus in paddy rice 93-11 (rice in China cross-breeding center, China, Changsha) by infestation method.Callus after will infecting is then grown on the screening culture medium that contains Totomycin (50mg/L), obtains the hygromycin resistance regeneration plant.

Getting hygromycin resistance regeneration plant blade is material, extracts genomic dna, is template with it, and the following primer that designs according to hygromycin gene carries out the PCR checking:

pC13-hyg-F：5’-ACCTGCCTGAAACCGAACTG-3’；

pC13-hyg-R：5’-CTGCTCCATACAAGCCAACC-3’。

Qualification result as shown in figure 10,1,2,3,4,5,6,12,13,15,16,18,20 the amplification of totally 12 strains system obtain the purpose band, promptly transformed plant T0 has 12 positive plants (being incorporated in the rice genome with the closely linked hygromycin gene of OsXCL) in generation.

2, check and analysis

Above-mentioned commentaries on classics OsXCL paddy rice is moved to hot-house culture, bagging selfing, the seed of collection transgenic paddy rice.

Be the empty carrier contrast to change the paddy rice that does not contain OsXCL expression carrier 163-1300 simultaneously; With the non-transgenic paddy rice equally in contrast.

1) quantitative PCR detection

Use OsXCL gene DNA sequence primer 108-F and 108-R, to change the OsXCL paddy rice, the non-transgenic paddy rice carries out quantitative PCR detection, the result as shown in figure 11, OsXCL expresses that level is very low relatively among the non-transgenic paddy rice 93-11; And the expression amount that changes OsXCL in the OsXCL paddy rice is significantly increased.

Wherein, the RT-PCR primer is as follows:

108-F：5’-CCGCCATCATCCAAACTGA-3’(Tm?59，PCR?56)；

108-R：5’-GGTGACCACGCCCTTCTTC-3’(Tm?59，PCR?56)。

The RT-PCR system

Reagent	Concentration.	Volume (ul)	Volume (ul)	Final concentration (uM)
							+RT	-RT
2x Master reaction solution	2x	5.0	5.0	1x
					QuantutyTec?RT?mix	100x	0.1	0.0
The 108-F primer	20.0uM	0.2	0.2	0.4
					The 108-R primer	20.0uM	0.2	0.2	0.4
RNA-free water		0.5	0.6
					Template ribonucleic acid	5ng/ul	4.0	4.0	The 20ng/ reaction

					Always		10.0	10.0

The PCR recycle ratio The solubility curve condition

48℃/30min，1cycle 95℃/15sec

95℃/10min，1cycle 60℃/20sec

95℃/15sec，56℃/1min，40cycles 95℃/15sec

2) phenotype is observed and statistics

A. 100-grain weight and the grain length of the T0 of OsXCL trans-genetic hybrid rice 93-11, empty carrier contrast and non-transgenic paddy rice 93-11 for plant seed changeed in weighing respectively.

Experiment repeats 3 times, and the result is shown in Figure 12 and table 1, and 100-grain weight of commentaries on classics OsXCL paddy rice and grain length contrast with empty carrier with non-transgenic paddy rice 93-11 and compare, and show a marked increase.Wherein, change the 100-grain weight of OsXCL paddy rice and compare fresh weight increase by 25.1% with the wild-type paddy rice, dry weight increases by 23%, and grain increases by 1/4, and chalk rice rate reduces (raising of rice matter).

Table 1.T0 is for the 100-grain weight and the grain length of plant seed

	Change the OsXCL paddy rice	The empty carrier contrast	The non-transgenic paddy rice
				Grain length (mm)	11.3833±0.08868	8.7027±0.08997	8.6167±0.07836
100-grain weight (fresh weight) (g)	4.224±0.11	3.401±0.08	3.377±0.10
				100-grain weight (dry weight) (g)	3.36±0.09	2.761±0.07	2.73±0.09

Annotate: the seed dry weight is that seed was placed the quality of weighing and obtaining 3 days down at 37 ℃.

B. observe and add up the plant number of T0 for the plant leaf convolution.

The T0 that changes the OsXCL paddy rice contrasts with empty carrier with the non-transgenic paddy rice for plant leaf and compares, plant leaf is slightly wide, plant sword-like leave convolution is (Figure 13) obviously, the ratio that the plant that contains the convolution leaf accounts for the plant that changes the OsXCL paddy rice reaches 90%, and begin to curl from blade base, to development later stage, top trails.

Sequence table

＜110〉Xiaxin circle

＜120〉with relevant albumen and encoding gene and the application of paddy rice long grain leaf roll

<130>CGGNARL92496

<160>2

<210>1

<211>1062

<212>DNA

＜213〉paddy rice (Oryza sativa)

<400>1

ctcacacacc?acaccacacc?aacatcgagc?gcgtcgagtc?gaatccaatc?cactccactc 60

caccccgcga?tctcctctcc?tctcgtctcc?ggcgaagacg?acgtgatgcc?acccagcgcc 120

gccgccgcag?ccgcgatggc?gcagtcgccg?cgcagcctcc?acacgctgat?cagcttcggc 180

cgcggcgccg?acggcgtcga?cgacgatgag?gccacgcccg?cgtcggtcga?cgttggtgac 240

gcggagggcg?ccgggctcga?cctcgacttc?gcgttcgcgc?cgccggtgtc?ggcggccgag 300

ctggcgccgg?ccgacgacat?cttcgcgcac?ggccgcatcg?tgccggcgta?cccggtgttc 360

gaccgcagcc?tcctcgacct?ctcgcccggc?gacgcctcca?cggcggcgcc?ctccgccgac 420

acctactgcg?cgtggacgcc?gcgctcggcg?ccgggctcgc?ccggccgcga?caggttcccc 480

aagagcgcgt?ccaccggcgg?agagtcgtcg?tcgtcatcgc?ggcgctggcg?cctgcgcgac 540

ctcgtcggcg?ccggcggccg?ctcccgcagc?gacggcaagg?acaagttcgc?cttcctgcac 600

caccacgccg?ccgcgccgcc?atcatccaaa?ctgaagactc?ctcctccccc?tcaacaacca 660

cagcagaaga?agcagagcgc?cgtgaagacg?aagccggcgg?cgaagaaggg?cgtggtcacc 720

gagatggaca?tggccaccgc?gcacaggctc?ttctacagca?aggccagcgc?cggcggcgac 780

cggcggccgc?agcaagcctc?gtacctgacg?taccgaccgg?cgttcagcgg?cctcttcgcg 840

ctcggccggt?cgcaacacca?caccgcctat?tagtttaatc?acttggtcaa?taaccaaacc 900

aactgattac?tagtggtagt?tgttgttaaa?ttaattgttt?tgttgtaaaa?gtgttcaaaa 960

ttttcggcga?aattcgagtc?gagatttctc?gtttgtacta?gaaccttatc?atgtacataa 1020

atggaaaaag?agaggaatga?aatttgagag?atgattttgt?ct 1062

<210>2

<211>255

<212>PRT

＜213〉paddy rice (Oryza sativa)

<400>2

Met?Pro?Pro?Ser?Ala?Ala?Ala?Ala?Ala?Ala?Met?Ala?Gln?Ser?Pro?Arg

1 5 10 15

Ser?Leu?His?Thr?Leu?Ile?Ser?Phe?Gly?Arg?Gly?Ala?Asp?Gly?Val?Asp

20 25 30

Asp?Asp?Glu?Ala?Thr?Pro?Ala?Ser?Val?Asp?Val?Gly?Asp?Ala?Glu?Gly

35 40 45

Ala?Gly?Leu?Asp?Leu?Asp?Phe?Ala?Phe?Ala?Pro?Pro?Val?Ser?Ala?Ala

50 55 60

Glu?Leu?Ala?Pro?Ala?Asp?Asp?Ile?Phe?Ala?His?Gly?Arg?Ile?Val?Pro

65 70 75 80

Ala?Tyr?Pro?Val?Phe?Asp?Arg?Ser?Leu?Leu?Asp?Leu?Ser?Pro?Gly?Asp

85 90 95

Ala?Ser?Thr?Ala?Ala?Pro?Ser?Ala?Asp?Thr?Tyr?Cys?Ala?Trp?Thr?Pro

100 105 110

Arg?Ser?Ala?Pro?Gly?Ser?Pro?Gly?Arg?Asp?Arg?Phe?Pro?Lys?Ser?Ala

115 120 125

Ser?Thr?Gly?Gly?Glu?Ser?Ser?Ser?Ser?Ser?Arg?Arg?Trp?Arg?Leu?Arg

130 135 140

Asp?Leu?Val?Gly?Ala?Gly?Gly?Arg?Ser?Arg?Ser?Asp?Gly?Lys?Asp?Lys

145 150 155 160

Phe?Ala?Phe?Leu?His?His?His?Ala?Ala?Ala?Pro?Pro?Ser?Ser?Lys?Leu

165 170 175

Lys?Thr?Pro?Pro?Pro?Pro?Gln?Gln?Pro?Gln?Gln?Lys?Lys?Gln?Ser?Ala

180 185 190

Val?Lys?Thr?Lys?Pro?Ala?Ala?Lys?Lys?Gly?Val?Val?Thr?Glu?Met?Asp

195 200 205

Met?Ala?Thr?Ala?His?Arg?Leu?Phe?Tyr?Ser?Lys?Ala?Ser?Ala?Gly?Gly

210 215 220

Asp?Arg?Arg?Pro?Gln?Gln?Ala?Ser?Tyr?Leu?Thr?Tyr?Arg?Pro?Ala?Phe

225 230 235 240

Ser?Gly?Leu?Phe?Ala?Leu?Gly?Arg?Ser?Gln?His?His?Thr?Ala?Tyr

245 250 255

Claims

1. an albumen is following 1) or 2) albumen:

2. the described proteic encoding gene of claim 1.

3. gene according to claim 2 is characterized in that: described gene is following 1) or 2) or 3) or 4) gene:

3) under the rigorous condition of height with 1) or 2) gene recombination and the described proteic gene of coding claim 1 that limit;

4) with 1) or 2) gene that limits has the homology 90% or more and the described proteic gene of claim 1 of encoding.

4. the transgenic cell line or the reorganization bacterium that contain claim 2 or 3 described genes.

5. the recombinant vectors that contains claim 2 or 3 described genes.

6. recombinant vectors according to claim 5 is characterized in that, described recombinant vectors is the multiple clone site with claim 2 or 3 described genes insertion expression vector 163-1300, the recombinant vectors that obtains;

7. cultivating the heavily method of the transgenic plant of increase of grain for one kind, is that claim 2 or 3 described genes are imported the purpose plants, obtains transgenic plant, and the grain of described transgenic plant is great in described purpose plant.

8. a method of cultivating long grain leaf roll transgenic plant is that claim 2 or 3 described genes are imported the purpose plant, obtains transgenic plant, and the grain length of described transgenic plant is greater than described purpose plant.

9. according to claim 7 or 8 described methods, it is characterized in that: claim 2 or 3 described genes are to import in the purpose plant by claim 5 or 6 described recombinant vectorss.

10. according to the arbitrary described method of claim 7-9, it is characterized in that: described plant is dicotyledons or monocotyledons; Described monocotyledons is a paddy rice.